76165-50-9

Upstream product

• 874-60-2 4-methyl-benzoyl chloride 
• 106-50-3 1,4-phenylenediamine 
• 624-18-0 benzene-1,4-diamine hydrochloride 
• 64-19-7 acetic acid 
• 76165-20-3 N,N′-(cyclohexa-2,5-diene-1,4-diylidene)bis-(4-methylbenzamide) 

Downstream Products

• 76165-55-4 N,N'-di-p-toluoyl-2,5-dichloro-1,4-diphenylenediamine 
• 76165-40-7 2,5-dichloro-N,N'-di-p-toluoyl-p-benzoquinone diimine 
• 76165-51-0 2-chloro-N,N'di-p-toluoyl-p-phenylenediamine 
• 76165-29-2 2-chloro-N,N'-di-p-toluoyl-p-benzoquinone diimine 
• 76165-20-3 N,N′-(cyclohexa-2,5-diene-1,4-diylidene)bis-(4-methylbenzamide) 

Relevant academic research and scientific papers

N,N'-bis(4-methylbenzoyl)-p-phenylene-diamine at 200 K

The title compound, N,N'-p-phenylenebis(4-methylbenzamide), C22H20N2O2, crystallizes with an almost linear arrangement of the three benzene units, but both outer benzene ring planes are twisted relative to the plane of the central ring by 58.03 (6)°. N-H...O=C hydrogen bonds perpendicular to the long axis of the molecules connect them into ribbons parallel to the a axis.

Reaction of N,N′-disubstituted 1,4-benzoquinone diimines with sodium arenesulfinates

Radical anion 1,6-addition path in the reactions of N,N′-disubstituted 1,4-benzoquinone diimines with sodium arenesulfinates is favored by increase of the electron-donating power of the substituent in the para position of arenesulfinate ion and redox pote